Total synthesis and assignment of the absolute stereochemistry of xanthoangelol J: development of a highly efficient method for Claisen–Schmidt condensation
D Kakati, NC Barua
Index: Kakati, Dwipen; Barua, Nabin C. Tetrahedron, 2014 , vol. 70, # 3 p. 637 - 642
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Citation Number: 3
Abstract
Abstract The first total synthesis of cancer chemopreventive terpenyl hydroxychalcone xanthoangelol J isolated from Angelica keiskei was accomplished with asymmetric epoxidation, aromatic C-alkylation and Claisen–Schmidt condensation via enol mode as key steps. The crucial Claisen–Schmidt condensation has been accomplished by a novel green method using KHSO 4–SiO 2 as a recyclable catalyst under microwave activation. The ...
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